Canonical Allele Identifier: CA398317025
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131244C>A (hg19) chr17:g.27804218C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804218C>A , CM000679.2:g.27804218C>A GRCh38
NC_000017.10:g.26131244C>A , CM000679.1:g.26131244C>A GRCh37
NC_000017.9:g.23155371C>A NCBI36
NG_011470.1:g.1312G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.343G>T ENSP00000462879.1:p.Gly115Trp
XM_011524859.1:c.-169G>T XP_011523161.1:n.-169G>T
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